Canonical Allele Identifier: PA238327
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.His786Gln
CA238324
NM_133378.4:c.2358C>G
CA349499544
NM_133378.4:c.2358C>A